KMID : 0191120230380120091
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Journal of Korean Medical Science 2023 Volume.38 No. 12 p.91 ~ p.91
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Tiotropium Bromide Improves Neutrophilic Asthma by Recovering Histone Deacetylase 2 Activity
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An Tai-Joon
Kim Ji-Hye Hur Jung Park Chan-Kwon Lim Jeong-Uk Kim Seo-Hyun Rhee Chin-Kook Yoon Hyoung-Kyu
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Abstract
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Background : The value of tiotropium bromide (TIO) in neutrophilic asthma was meaningful in previous study. We hypothesized that TIO¡¯s mechanism of action is associated with histone deacetylase 2 (HDAC2) activity, which is key for controlling the transcription of inflammatory cytokines and usually downregulated in neutrophilic asthma.
Methods : The effects of TIO and dexamethasone (DEX) on HDAC2 activity, nuclear factor kappa B (NF-¥êB), and C-X-C motif chemokine ligand 1 (CXCL1) were evaluated in neutrophilic asthma mouse model (C57BL, 6-week-old). An in-vitro study was conducted using primary human bronchial/tracheal epithelial (HBE) cells from asthma patients. Western blot analyses were performed for phospho-phospholipase C¥ã-1 (PLC¥ã-1) and inositol trisphosphate (IP3) receptors (IP3R) with treating lipopolysaccharide (LPS) and TIO.
Results : Ovalbumin was used to induce eosinophilic inflammation in this study. After neutrophilic asthma was induced by LPS (O+L group), HDAC2 activity was diminished with increased NF-¥êB activity and CXCL1 compared to the control group. TIO significantly improved NF-¥êB activity, CXCL1, and HDAC2 activity compared with the O+L group in in-vivo study (P < 0.05, each). Western blot analyses showed that LPS treated HBE cells from asthma patients increased PLC¥ã-1 and diminished IP3 receptor levels. After TIO treatment, recovery of IP3R and improved PLC¥ã-1 levels were observed.
Conclusion : These results support the hypothesis that TIO modulates inflammation by recovering HDAC2 activity from the acetylcholine-stimulated inflammation cascade in neutrophilic asthma. The detailed inflammation cascade of recovering HDAC2 activity by TIO might be associated with PLC¥ã-1-IP3-IP3R mediated intracellular calcium ion pathway.
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KEYWORD
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Asthma, Neutrophils, Tiotropium bromide, Histone Deacetylases 2
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